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Infection and Immunity, October 2004, p. 6068-6075, Vol. 72, No. 10
0019-9567/04/$08.00+0     DOI: 10.1128/IAI.72.10.6068-6075.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

The Streptococcus pyogenes Capsule Is Required for Adhesion of Bacteria to Virus-Infected Alveolar Epithelial Cells and Lethal Bacterial-Viral Superinfection

Shigefumi Okamoto,¹ Shigetada Kawabata,^1,2* Yutaka Terao,¹ Hideaki Fujitaka,¹ Yoshinobu Okuno,³ and Shigeyuki Hamada¹

Department of Oral and Molecular Microbiology, Osaka University Graduate School of Dentistry, Suita-Osaka,¹ PRESTO, Japan Science and Technology Agency, Kawaguchi-Saitama,² Department of Infectious Diseases, Osaka Prefectural Institute of Public Health, Osaka, Japan³

Received 21 October 2003/ Returned for modification 10 June 2004/ Accepted 14 July 2004

Top Abstract Introduction Materials and Methods Results Discussion References

 
An apparent worldwide resurgence of invasive group A Streptococcus (GAS) infections remains unexplained. However, we recently demonstrated in mice that when an otherwise nonlethal intranasal GAS infection is preceded by a nonlethal influenza A virus (IAV) infection, induction of lethal invasive GAS infections is often the result. In the present study, we established several isogenic mutants from a GAS isolate and evaluated several virulence factors as candidates responsible for the induction of invasive GAS infections. Disruption of the synthesis of the capsule, Mga, streptolysin O, streptolysin S, or streptococcal pyrogenic exotoxin B of GAS significantly reduced mortality among mice superinfected with IAV and a mutant. In addition, the number of GAS organisms adhering to IAV-infected alveolar epithelial cells was markedly reduced with the capsule-depleted mutant, although this was not the case with the other mutants. Wild-type GAS was found to bind directly to IAV particles, whereas the nonencapsulated mutant showed much less ability to bind. These results suggest that the capsule plays a key role in the invasion of host tissues by GAS following superinfection with IAV and GAS.

Top Abstract Introduction Materials and Methods Results Discussion References

 
Streptococcus pyogenes (group A Streptococcus [GAS]) is known to be the cause of such diseases as uncomplicated pharyngitis, impetigo, and acute rheumatic fever (10). In addition, severe invasive GAS infections, leading to a wide range of diverse diseases that include acute respiratory distress syndrome, renal failure, streptococcal toxic shock syndrome, sepsis, and cellulitis, have been reported in North America, Europe, and Japan (4, 23, 30, 35, 41). GAS invades the host via the upper respiratory tract or injured skin surfaces (10). Although many invasive GAS isolates are reportedly of the M1 or M3 serotype, which produce streptococcal pyrogenic exotoxin A (10), the reasons for the recent emergence, or reemergence, of invasive GAS infections remain unknown.

Statistically, the incidence of GAS infections is highest in winter, when influenza epidemics are common (5, 12, 28). In that regard, we recently used a mouse model to show that superinfection with influenza A virus (IAV) and GAS applied intranasally causes a lethal GAS infection that affects various tissues and organs of the host (32). In that study, GAS organisms adhered to the surface of IAV-infected alveolar epithelial cells of superinfected mice, although no GAS adhered to epithelial cells of mice infected with GAS alone. Moreover, our electron microscopic observations confirmed that GAS organisms bind directly to IAV particles on the cell surfaces. Taken together, these results suggest that IAV infection plays a key role in the enhanced internalization of GAS by alveolar epithelial cells, resulting in the emergence of sepsis and other invasive GAS diseases. Beyond this, however, little is known about the mechanisms via which invasive IAV-GAS superinfections occur.

Ashbaugh et al. (3) established a murine model of human necrotizing fasciitis and concluded that the GAS hyaluronic acid capsule and M protein, but not the cysteine protease streptococcal pyrogenic exotoxin B (SPEB), are critical for the development of tissue necrosis, secondary bacteremia, and eventually death. In addition, another GAS virulence factor, streptolysin O (SLO), which binds to cholesterol in red blood cell membranes, causing lysis, reportedly exerts various neurological effects, increases capillary permeability, and induces dermal necrosis in rabbits (1). On the other hand, direct studies of the role of SLO during infection recently revealed that the contribution of SLO to GAS virulence was limited in a murine dermonecrosis invasive infection model (26). Still another factor is streptolysin S (SLS), which like SLO is potently cytolytic (1). These findings raise questions as to the respective contributions made by the various GAS virulence factors to the induction of invasive infections with otherwise nonlethal doses of IAV and GAS. In the present study, genes encoding hyaluronic acid capsule, M protein, SLO, and SLS were inactivated by allelic replacement. We then examined the mortality among mice superinfected with IAV and wild-type strain SSI-9 or one of its isogenic mutant strains.

Top Abstract Introduction Materials and Methods Results Discussion References

 
Virus, bacteria, mice, and cell line. IAV A/FM/1/47 (H1N1) (34) was suspended in phosphate-buffered saline (PBS) before use in all subsequent studies. The bacterial strains and plasmids used in this study are listed in Table 1. GAS strain SSI-9 (M1) was an isolate from a Japanese patient with severe invasive fasciitis and was provided by T. Murai (Toho University, Tokyo, Japan). For selection of GAS mutants, the organisms were grown in Todd-Hewitt broth supplemented with 0.2% yeast extract (THY) (Difco Laboratories, Detroit, Mich.) for 6 h at 37°C (31, 33), after which kanamycin (500 µg/ml) or spectinomycin (1 mg/ml) was added to the medium. Female BALB/c mice (H-2^d, 8 weeks old, 18 to 20 g) were purchased from Charles River Inc. (Yokohama, Japan). A human alveolar epithelial cell line, A549, was grown in RPMI 1640 medium (Sigma, St. Louis, Mo.) supplemented with 10% fetal bovine serum (FBS) (Gibco-BRL, New York, N.Y.).

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TABLE 1. Bacterial strains and plasmids used in this study

Mutagenesis using targeted plasmids and characteristic measurements of hasA, speB, slo, and sagA mutants. PCR with specific primer sets (Table 2) was used to amplify gene fragments from the hasA, speB, slo, and sagA genes, encoding hyaluronate synthase, SPEB, SLO, and SLS, respectively. The PCR products were ligated into pGEM-T Easy vectors (Promega, Madison, Wis.) and digested with EcoRI, after which the fragments were cloned into vectors as described in Table 1. The resultant plasmids, pIN151, pTM16, and pYT1111, were transformed into GAS strain SSI-9 by electroporation, yielding the mutants TR-10 (slo), TR-11 (speB) and TR-17 (sagA), respectively (Fig. 1A and Table 1). The inactivated mutant strains were then selected by using kanamycin- or spectinomycin-containing agar plates. An hasA-inactivated mutant, TR-8, was constructed in the same way by first constructing E-1, as described previously (24); likewise, TR-5 was constructed as described previously (43, 45).

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TABLE 2. PCR primer sets used for targeted mutagenesis

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FIG. 1. Targeted mutagenesis of slo in GAS strain SSI-9. (A) pIN151 contains an internal fragment of slo and a kanamycin resistance gene (aphA3). TR-10 was produced by a single-crossover recombination. The speB (TR-11) and sagA (TR-17) mutants were constructed in a similar fashion. (B) The hasA, slo, speB, and sagA mutants were subjected to PCR with a targeted gene-specific forward primer and an aphA3- or aad9-specific reverse primer. (C) Strain SSI-9 and its mutants (107 CFU per 50 µl) were inoculated into 5 ml of THY broth and incubated at 37°C. Growth was determined by measuring the optical density at 600 nm (OD600).

Detection of hyaluronic acid and sialic acid. GAS-associated hyaluronic acid was removed from GAS organisms, and the uronic acid content was quantitated as described by Schranger et al. (39). Hyaluronic acid from S. zooepidemicus (Wako, Osaka, Japan) was used as the standard. Detection of capsular polysaccharide from GAS was performed as described previously (50), and the sialic acid content was estimated by using the thiobarbituric acid method (48).

Caseinolytic assay. The proteolytic activity of SPEB was assessed by using a casein agar plate assay as described previously (7). Briefly, the test strain was inoculated onto THY agar plates containing 10% skim milk (Difco). The plates were then incubated for 48 h at 37°C in an anaerobic GasPak (Becton Dickinson, Mountain View, Calif.). Caseinolytic activity resulted in a zone of translucence surrounding the stab site.

Hemolytic assays. SLO hemolytic assays were carried out essentially as described by Limbago et al. (26). Briefly, an overnight culture of test strains was adjusted to an absorbance of 1.0 at 600 nm, after which the supernatant was separated by centrifugation for 10 min at 7,500 x g and then filtered (pore size, 0.25 µm). The cleared supernatant was incubated for 10 min at room temperature with 10 mM dithiothreitol, after which two 0.5-ml aliquots of each sample were placed in 1.5-ml sterile tubes, and 25 µl of cholesterol (Sigma) was added to one of the aliquots. Following a 30-min incubation at 37°C, 0.25 ml of a 2% suspension of bovine erythrocytes in PBS was added to each aliquot, mixed by inversion, and incubated for 30 min at 37°C. Finally, 0.5 ml of PBS was added to each sample, and intact erythrocytes were collected by centrifugation for 1 min at 200 x g. Supernatants were then removed, and the release of hemoglobin was assessed by reading the absorbance at 541 nm.

SLS hemolytic assays were carried out as described by Sierig et al. (40). Test organisms were grown for 16 h in brain heart infusion broth supplemented with 2% Na₂CO₃ and 1% maltose. They were then washed in 100 mM potassium phosphate buffer (pH 7.0), after which 4 mg (dry weight) of the organism were suspended in 1 ml of 100 mM KPB (pH 7.0) containing 2 mM MgSO₄ and 30 mM maltose. The suspension was incubated for 5 min at 37°C, induced by treatment with 0.5 mg of RNA core (Sigma) for 5 min, and centrifuged at 15,000 x g and 4°C for 20 min. The resultant supernatant was collected, and ammonium acetate (100 mM final concentration) was added to stabilize SLS. After preparation of a standardized suspension of sheep erythrocytes comprised of PBS (pH 6.5) containing 6% defibrinated sheep blood and 0.1% bovine serum albumin (BSA) (Sigma), 1 ml of the supernatant was incubated with 0.5 ml of the standardized erythrocyte suspension for 45 min at 37°C. Intact erythrocytes were removed by centrifugation, and release of hemoglobin was assessed by reading the absorbance at 541 nm.

Microbial infections and counting of microorganisms in internal organs. To examine the lethality of superinfection with IAV and GAS, mice were intranasally administrated 25 µl of PBS with or without 100 focus-forming units (FFU) of IAV, followed 2 days later by intranasal administration with 25 µl of PBS containing 10⁷ CFU of GAS. To determine the number of GAS organisms present in the lungs, liver, spleen, and kidneys, the organs were dissected and homogenized in PBS, after which 10-fold dilutions of each suspension were plated on THY blood agar plates, and colonies were counted after incubation overnight at 37°C (11).

Histopathology. Tissue samples were fixed in 10% (vol/vol) neutral phosphate-buffered formalin and embedded in paraffin. Sections were cut to a thickness of 6 µm. For GAS and IAV hemagglutinin (HA)-expressed cell detection, sections were stained with rabbit GAS strain SSI-9 antiserum (29) and fluorescein isothiocyanate-conjugated anti-rabbit immunoglobulin G and/or Alexa Fluor 568 (Molecular Probes, Eugene, Oreg.)-conjugated anti-IAV HA monoclonal antibody (MAb). Each section was assigned a number, which enabled unbiased examination with a model LSM 510 confocal microscope (Carl Zeiss, Oberkochem, Germany).

Assays for GAS adhesion and invasion. Assays for GAS adhesion to or invasion of epithelial cells were carried out as described previously (32). Briefly, IAV (2 x 10⁶ FFU) was inoculated onto semiconfluent A549 cell monolayers (10⁵ cells) in 24-well culture plates and incubated with 200 µl of RPMI 1640 medium (pH 6.0) containing 0.2% BSA for 30 min at 37°C in 5% CO₂ (34). The medium was then aspirated and replaced with fresh medium (1 ml/well), and the cells were incubated for 17 h at 37°C in 5% CO₂. Thereafter, the cells were washed twice, inoculated with fresh GAS organisms (10⁶ CFU) suspended in 200 µl of medium, and incubated for 2 h at 37°C in 5% CO₂. Unattached bacteria were then removed by washing with PBS, and A549 cells were disrupted and serially diluted by addition of sterile distilled water and plated on THY agar plates to determine the total number of GAS organisms associated with the epithelial cells (24, 32).

For the invasion assay, GAS organisms (10⁶ CFU/200 µl of conditioned medium) were incubated with cell monolayers for 2 h at 37°C in 5% CO₂. Unattached bacteria were removed by washing with 1 ml of PBS, and the GAS organisms associated with the cell surface were killed by treatment with gentamicin (100 µg/ml) and penicillin (10 U/ml) for 1 h. The cell monolayers were then washed, disrupted with sterile distilled water, serially diluted in water, and plated on THY agar plates to determine the number of internalized GAS bacteria (24, 32).

Measurement of binding of GAS organisms to IAV particles. IAV particles were suspended in PBS containing 0.2% BSA, after which an aliquot of IAV (0.5 ml) or PBS containing 0.2% BSA (0.5 ml) was added to the wells of a six-well multiplate (36, 49) and incubated overnight at 4°C. The wells were then washed three times with PBS, GAS organisms (5 x 10⁶ CFU in 0.5 ml of PBS) were added, and the plate was incubated for an additional 1 h at 4°C. After washing six times with PBS, PBS containing 0.5% Triton X-100 (1 ml/well) was added to the wells and then incubated for 30 min at room temperature to remove adherent GAS. Tenfold dilutions of each suspension were plated on THY blood agar plates, and the colonies were counted after incubation overnight at 37°C. In parallel experiments, GAS organisms (10⁹ CFU) were treated with neuraminidase (0.6 U per 0.5 ml of 50 mM sodium acetate supplemented with 0.9% NaCl and 0.1% CaCl₂) for 3 h at 37°C to remove the sialic acid.

Statistical evaluations. Fisher's exact test was carried out by using StatView software (SAS Institute Inc., Cary, N.C.) to evaluate differences between groups in the mortality experiments. To analyze data from other experiments, nonparametric Mann-Whitney U tests and Wilcoxon two-sample rank tests were used. P values of <0.05 were considered significant.

Top Abstract Introduction Materials and Methods Results Discussion References

 
Targeted mutagenesis of hasA, slo, speB, and sagA. Targeted inactivation of hasA, slo, speB, and sagA in GAS strain SSI-9 resulted in the generation of mutants TR-8, TR-10, TR-11, and TR-17, respectively. Each mutation was confirmed by PCR analysis of the chromosomal DNA with targeted gene-, aphA3-, and aad9-specific primers. Fragments spanning the region between the targeted gene and aphA3 or aad9 were amplified by using the appropriate primer pairs (Fig. 1B), and it was confirmed that only a single insert was present in the chromosome and that no transcript was made from the resultant gene (data not shown). Thus, all targeted genes were inactivated in these mutants. We assessed the growth rates of SSI-9 and its mutants and confirmed that the presence of an antibiotic cassette in the chromosome did not cause a lower growth rate (Fig. 1C).

Hyaluronic acid expression, caseinolysis, and hemolysis were measured to determine the degree to which mutation of hasA, speB, slo, and sagA had affected their activities. Quantitative chemical analysis revealed that TR-8, the hasA mutant, produced no detectable cell-associated hyaluronate. By contrast, the other strains synthesized almost 30 fg of hyaluronate per CFU (Table 3). We also confirmed that TR-11, the speB mutant, showed markedly reduced caseinolytic activity, while TR-10, the slo mutant, and TR-17, the sagA mutant, showed markedly reduced levels of SLO- or SLS-dependent hemolytic activity (Table 3).

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TABLE 3. Characteristics of wild-type and mutant strains of GAS used in this studya

Effect of isogenic GAS mutagenesis on mortality among mice subjected to viral-bacterial superinfection. Alone, IAV at a dose of 100 FFU or GAS at a dose of 10⁷ CFU did not induce a lethal infection in mice (32). On the other hand, prior infection with 100 FFU of IAV markedly increased mortality following inoculation with GAS (Fig. 2). Using the same experimental protocol, we then examined the effect on mouse mortality of the individual GAS virulence factors. The mortality among mice infected with SSI-9 mutants following IAV infection was significantly diminished, from 90% with wild-type strain SSI-9 to less than 60% for each of the mutants (Fig. 2). Notably, the most pronounced reduction in mortality rate (to only about 20%) was seen with the hasA-inactivated TR-8 mutant, which is consistent with the finding that among the six organisms tested, the TR-8 mutant exhibited the lowest levels in lung 24 h after infection (Fig. 3A). Moreover, levels of TR-8 were also significantly lower than those of wild-type SSI-9 in several other organs 72 h after superinfection (Fig. 3B).

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FIG. 2. Mortality among mice superinfected with IAV and the indicated GAS test strain. Groups of 30 mice were intranasally infected first with IAV (100 FFU) in 25 µl of PBS on day –2 and then with SSI-9 or one of its mutant strains (107 CFU) in 25 µl of PBS on day 0. Mortality was assessed daily for 10 days after GAS infection. Fisher's exact test was used to determine significant differences in mortality among the groups: P = 0.0012, P < 0.0001, P = 0.0127, P = 0.0470, and P = 0.0061, respectively, for TR-5, TR-8, TR-10, TR-11, and TR-17 versus SSI-9.

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FIG. 3. Effect of capsule removal on the number of GAS organisms in the internal organs of superinfected mice. (A) Ten mice were intranasally infected first with IAV (100 FFU) on day –2 and then with GAS strains (107 CFU) on day 0. The number of GAS organisms in the lungs was assessed on day 1. Circles under the broken line indicate that GAS was not detectable. Horizontal bars indicate the median values. Wilcoxon two-sample rank tests were used to evaluate the differences between groups: P = 0.1403, P = 0.0003, P = 0.1032, P = 0.2718, and P = 0.0880, respectively, for TR-5, TR-8, TR-10, TR-11, and or TR-17 versus SSI-9. (B) The numbers of GAS organisms in the lungs, livers, spleens, and kidneys of mice superinfected with IAV and SSI-9, or TR-8 were determined on days 1 and 3. Circles under the broken line indicate that GAS was undetectable. Horizontal bars indicate the median values. Mann-Whitney U tests were used to evaluate differences between groups *, P < 0.01; **, P < 0.05.

Adhesion and invasion of IAV-infected epithelial cells by isogenic GAS mutants. GAS organisms in the lungs of superinfected mice bind to IAV-infected alveolar epithelial cells (32). However, the fluorescence micrographs in Fig. 4 show that the numbers of GAS organisms associated with IAV-infected alveolar epithelial cells in the superinfected mice were diminished by inactivation of hasA. We also observed significantly less adhesion to and invasion of cultured A549 cells when they were infected with IAV and TR-8 than when they were infected with IAV and SSI-9 (Fig. 5). Collectively, then, the results presented so far strongly suggest that the GAS capsule is crucial for the enhanced adhesion to and invasion of IAV-infected epithelial cells by GAS.

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FIG. 4. Association of GAS with IAV-infected alveolar epithelial cells. Mice were infected with SSI-9 or superinfected with IAV and SSI-9 or TR-8 as described in the legend to Fig. 2. Lungs were harvested 48 h after GAS infection, and sections were stained with Alexa Fluor 568-conjugated anti-HA MAb or rabbit polyclonal anti-GAS antibody and fluorescein isothiocyanate-conjugated anti-rabbit immunoglobulin G.

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FIG. 5. Expression of capsule by GAS is required for maximal adhesion to and invasion of cultured IAV-infected A549 epithelial cells. A549 cells were infected with IAV for 17 h. After subsequent infection with SSI-9 or TR-8 for 2 h, the number of GAS organisms adhering to or invading the epithelial cells was assessed. Data are shown as means ± standard errors of the means from 12 wells (four independent experiments performed in triplicate). Mann-Whitney U tests were used to evaluate the differences between groups. *, P < 0.01.

Our earlier electron microscopic observations revealed that GAS organisms bind directly to IAV particles exposed on the surface of epithelial cells (32). Here we confirmed that the binding of SSI-9 to IAV-coated plates was more than sixfold greater than that to plates without IAV (Fig. 6A). Furthermore, the nonencapsulated TR-8 mutant exhibited a significantly lower level of binding to IAV particles than wild-type SSI-9 (Fig. 6A).

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FIG. 6. Direct binding of GAS to IAV particles and effect of the GAS capsule and sialic acid on direct binding. (A) Wild-type SSI-9 or hasA-inactivated TR-8 mutant bacteria were added to IAV-coated wells (4 µg of IAV per ml, suspended in PBS containing 0.2% BSA), after which GAS binding to IAV particles was quantitated. Data are shown as means ± standard errors of the means from nine wells (three independent experiments performed in triplicate). Mann-Whitney U tests were used to evaluate differences between groups. *, P < 0.01 versus binding of SSI-9 to uncoated wells. (B) GAS (SSI-9) and GBS (COH1; type III) bacteria were cultured in THY broth, capsular polysaccharides from 100 mg (dry weight) of GAS and GBS were harvested, and the amount of sialic acid was estimated. (C) SSI-9 organisms were pretreated with or without neuraminidase, and the direct binding assay was performed.

Treatment of IAV-infected epithelial cells with anti-IAV HA MAb suppressed the binding of GAS to the epithelial cells (32). Since IAV-HA binds to sialic acid, we determined whether sialic acid was included in the GAS capsule. As shown in Fig. 6B, GAS possessed only trace amounts of sialic acid. Furthermore, the binding activity of GAS to IAV was not inhibited by pretreatment with neuraminidase (Fig. 6C).

Top Abstract Introduction Materials and Methods Results Discussion References

 
Based on the hypothesis that microbial superinfections frequently accompanied a fatal outcome during the 1918 Spanish influenza epidemic, various attempts have been made to examine the interaction between influenza viruses and some bacteria in animal models (13, 16, 22, 25, 27, 32, 37). It is still unknown, however, which bacterial virulence factor(s) is important for the induction of invasive bacterial-viral superinfection. The present results indicate that the GAS capsule, SPEB, Mga, SLO, and SLS all participate in the induction of a lethal synergism.

We previously found that prior IAV infection enhances GAS internalization by alveolar epithelial cells (32). In the present study, therefore, we focused on which GAS virulence factor(s) is critical for that enhanced internalization. We found that depletion of the GAS capsule, but not Mga, SPEB, SLO, or SLS, reduced the number of GAS organisms in the lungs adhering to IAV-infected alveolar epithelial cells and regulated adhesion to and invasion of IAV-infected A549 cells by GAS. The wild-type GAS strain SSI-9 was found to bind directly to IAV particles, whereas the nonencapsulated TR-8 mutant showed much less ability to bind, suggesting that the GAS capsule plays a key role in the enhanced internalization of the organism by IAV-infected alveolar epithelial cells. On the other hand, nonencapsulation of GAS by transposon mutagenesis resulted in increased susceptibility to phagocytosis in human blood, even though the encapsulated wild-type strains survived (51). This leads us to hypothesize that the lower levels of nonencapsulated GAS present in the lungs may be due not only to diminished association with IAV-infected alveolar epithelial cells but also to higher levels of phagocytosis by alveolar phagocytes.

Insertion of an antibiotic cassette in the chromosome may play a role in decreased virulence. However, the growth rate of the mutants was nearly the same as that of SSI-9 (Fig. 1C), and the numbers of mutants, except TR-8, in lungs of the superinfected mice were the same as that of SSI-9 at 24 h after the superinfection (Fig. 3). Furthermore, hyaluronic acid expression in all of the mutant strains except TR-8, caseinolytic activity in all of the mutant strains except TR-11, and hemolytic activity in all of the mutant strains except TR-10 and TR-17 were completely conserved (Table 3). These results suggest that the simple presence of an antibiotic cassette in the chromosome of GAS does not lead to decreased virulence but rather that any changes in virulence are due to its insertion into key pathogenicity-determining genes.

Studies of the adhesion of GAS organisms to epithelial cells have implicated several bacterial surface molecules, including M protein (38), fibronectin-binding proteins (9, 31, 45, 47), and laminin-binding proteins (42, 46). In addition, some investigators have reported the capsule to be critical for pharyngeal colonization, resistance to phagocytosis, and virulence in experimental GAS infections (14, 20). For instance, inactivation of hasA blocked infection after intranasal inoculation in mice (19), and effective colonization and invasion of the pharynx by virulent GAS strains appear to require a specific interaction between the GAS capsule and CD44 (11). That the GAS capsule was also required for binding to IAV particles and IAV-infected alveolar cells suggests that the capsule may also play a novel pathogenic role in the induction of invasive GAS diseases following superinfection with otherwise nonlethal doses of IAV and GAS.

The mortality among mice superinfected with IAV and GAS was also reduced to various degrees by inactivation of mga, slo, speB, or sagA (Fig. 1). That these mutants produced capsular hyaluronic acid at levels similar to that seen in the parent strain SSI-9 (Table 3) suggests that the Mga regulon (which regulates expression of mrp/fcrA, emm, enn, scpA, and fbaA), SLO, SPEB, and SLS also act as virulence factors contributing to the induction of invasive GAS diseases. Notably, however, association of the organisms with IAV-infected epithelial cells (Fig. 3 and 4) and inflammation of the lungs (data not shown) were diminished only with the hasA mutant TR-8. We suggest that the binding of the GAS capsule to IAV surface molecules on IAV-infected epithelial cells is likely enhanced by the host inflammatory response to local tissue injury caused by SLO, SPEB, and SLS.

In the present study, nonencapsulation correlates with decreased invasion into A549 epithelial cells, though Jadoun et al. (20, 21) reported that a decreased capsule is associated with an increased uptake into epithelial cells in the presence of FBS. Depletion of the GAS capsule resulted in the exposure of several adhesins, especially fibronectin-binding proteins (45, 47), and it was suggested that the proteins induce enhanced internalization in the presence of fibronectin in FBS. Since FBS contains a component, termed ß inhibitor, that inhibits the infectivity and hemagglutinating activity of IAV of the H1 and H3 subtypes (2), our experiments regarding internalization were performed in the absence of FBS. Therefore, we consider that the opposite effect was due to the lack of fibronectin in our assay system.

It remains unclear which molecules on the IAV surface bind the GAS capsule. One intriguing finding was that direct binding to IAV by sialic acid in the group B Streptococcus (GBS) capsule is mediated by fusion with IAV HA (18). HA, a 75-kDa protein expressed on the surface of the virus (6), participates in the fusion between virus envelopes and the endosomes of virus-infected cells prior to viral invasion of the cytoplasm (8, 17, 44). This does not appear to be the case with IAV and GAS, as GAS was found to possess only trace amounts of sialic acid and pretreating GAS with neuraminidase did not inhibit binding activity (Fig. 6B and C). Thus, the IAV protein that interacts with the GAS capsule remains to be identified.

Recently, McCullers and Rehg (27) found a lethal synergism between influenza viruses and Streptococcus pneumoniae in a mouse model. They speculated that influenza infection, which triggers elaboration of inflammatory cytokines, may indirectly up-regulate adhesion molecules on epithelial cells, providing a receptor for bacterial adhesion and invasion. For example, infection by adenovirus increases adhesion of pneumococci via a mechanism that is independent of the expression of adenovirus surface proteins, suggesting that a cell surface receptor was up-regulated (15).

In summary, we have shown that the GAS capsule, which appears to mediate the binding of the bacterium to IAV molecules exposed on the surface alveolar epithelial cells, is crucial for induction of lethal invasive GAS infections following superinfection with otherwise nonlethal doses of IAV and GAS.

 
We thank T. Uehira for technical assistance.

This study was supported by grants from the Japanese Ministry of Health, Welfare, and Labor; PRESTO, Japan Science and Technology Agency; and the Japanese Ministry of Education, Culture, Sports, Science and Technology.

 
* Corresponding author. Mailing address: Department of Oral and Molecular Microbiology, Osaka University Graduate School of Dentistry, 1-8 Yamadaoka, Suita, Osaka 565-0871, Japan. Phone: 81-6-6879-2898. Fax: 81-6-6878-4755. E-mail: kawabata{at}dent.osaka-u.ac.jp.

Editor: V. J. DiRita

Top Abstract Introduction Materials and Methods Results Discussion References

 

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Infection and Immunity, October 2004, p. 6068-6075, Vol. 72, No. 10
0019-9567/04/$08.00+0     DOI: 10.1128/IAI.72.10.6068-6075.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

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